autosomal recessive nonsyndromic deafness 16
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the STRC gene on chromosome 15q15
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Summary
autosomal recessive nonsyndromic deafness 16 is a head and neck disease[1].
Key Facts
- autosomal recessive nonsyndromic deafness 16's instance of is recorded as head and neck disease[2].
- autosomal recessive nonsyndromic deafness 16's instance of is recorded as rare disease[3].
- autosomal recessive nonsyndromic deafness 16's instance of is recorded as class of disease[4].
- autosomal recessive nonsyndromic deafness 16 is a type of autosomal recessive nonsyndromic deafness[5].
- autosomal recessive nonsyndromic deafness 16's genetic association is recorded as STRC[6].
- autosomal recessive nonsyndromic deafness 16's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110471[7].
- autosomal recessive nonsyndromic deafness 16's exact match is recorded as http://identifiers.org/doid/DOID:0110471[8].
- autosomal recessive nonsyndromic deafness 16's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].